Home Chemistry Organic Building Blocks Esters Benzyl Benzylcarbamate
Transesterification: Benzyl benzylcarbamate can undergo transesterification reactions with other alcohols or carbamates, leading to the formation of different carbamates and alcohols.
Reduction: Benzyl benzylcarbamate can be reduced using various reducing agents to form benzylamine. Common reducing agents for this purpose include sodium borohydride (NaBH4) or lithium aluminum hydride (LiAlH4).
Acylation: Benzyl benzylcarbamate can be acylated at the carbamate nitrogen or the benzyl group to introduce various substituents. For instance, acylation with acid chlorides or anhydrides can lead to the formation of N-acylbenzyl benzylcarbamates.
Esterification: Benzyl benzylcarbamate can be esterified with carboxylic acids to produce various esters. This reaction typically involves the use of acid catalysts, such as sulfuric acid.
Dehydration: Under specific conditions, benzyl benzylcarbamate can undergo dehydration reactions to produce unsaturated compounds.
Oxidation: Depending on the reaction conditions, benzyl benzylcarbamate can be subject to oxidation, leading to the formation of various oxidized products.
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tert-Butyl 4-((((benzyloxy)carbonyl)amino)methyl)benzoate
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(R)-Benzyl (2-amino-1-phenylethyl)carbamate
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4-((((Benzyloxy)carbonyl)amino)methyl)benzoic acid
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(R)-4-(1-(((Benzyloxy)carbonyl)amino)ethyl)benzoic acid
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Benzyl 3-aminobenzylcarbamate hydrochloride
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(S)-(2-amino-1-phenyl-ethyl)-carbamic acid benzyl ester
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